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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111024Generated: November 1, 2026

Pyridine → HCID 57053574, compound

https://huagongshe.com/reaction/1111024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrimethyl orthoformateHCID 9005—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 86742137HCID 86742137—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57053574HCID 57053574—

Reaction Steps

A solution of 0.1 mol of 4-(allylamino)benzaldehyde ethylene glycol acetal in 100 mL of anhydrous THF is added dropwise over 10 minutes to a solution of 0.1 mol of the glycine phenyl ester isocyanate and 0.35 mol pyridine in 100 mL THF at room temperature under N2. The reaction mixture is stirred at room temperature for 2 hours. After 2 hours the solvent is removed by rotary evaporator. A solution of 0.1 mmol hydroxylamine hydrochloride and 0.1 mol trimethyl orthoformate in CH3OH is added, and the reaction mixture is heated to reflux under N2 for 1 hour. The reaction mixture is reduced to about 1/4 volume by rotary evaporator, and water is added. The product, N-allyl-N-4-(hydroxyiminomethyl)phenyl]-N'-phenoxycarbonylmethylurea, is isolated by filtration and dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977272
Source datasetuspto-grants-1990_12
ORD IDord-3a3463137b8d4fb3afb290067d229920
Source noteuspto-grants-1990_12